Photochromism of spiropyran nanocrystals embedded in sol-gel matrices.

Spectroscopic and kinetic properties of a new photochromic medium, consisting of nanocrystals of spyropyran molecules (1,3-dihydro-1,3,3,5',6',pentamethyl-spiro[2H-indole-2,2'-[2H]pyrano [3,2-b]pyridinium] iodide) embedded in an organo-silicate sol-gel film, are presented and compared to microcrystals obtained by slow evaporation of a solvent. High photoconversion efficiencies for both kinds of crystals have been observed. In microcrystals, the photomerocyanine form absorbs at 570 nm with a fading rate of 5 h, in nanocrystals the photomerocyanine form absorbs at 535 nm with a fading rate of 41 h. Therefore, the crystalline structure of nanocrystals is different from the microcrystal one.

In situ diagnostics of the crystalline nature of single organic nanocrystals by nonlinear microscopy.

We elucidate the crystalline nature and the three-dimensional orientation of isolated organic nanocrystals embedded in a sol-gel matrix, using a polarized nonlinear microscopy technique that combines two-photon fluorescence and second harmonic generation. This technique allows the distinction between monocrystalline structures and nanoscale polycrystalline aggregates responsible for incoherent second harmonic signals.